Canonical Allele Identifier: CA435815663

Gene: TF

Linked Data

• gnomAD v4: 3-133766408-C-T
• MyVariant Identifiers: chr3:g.133485252C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766408C>T , CM000665.2:g.133766408C>T	GRCh38
NC_000003.11:g.133485252C>T , CM000665.1:g.133485252C>T	GRCh37
NC_000003.10:g.134967942C>T	NCBI36
NG_013080.1:g.25276C>T
NG_013080.2:g.109411C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1461C>T MANE Select	ENSP00000385834.3:p.Tyr487=
ENST00000402696.7:c.1461C>T	ENSP00000385834.3:p.Tyr487=
ENST00000461695.1:c.131C>T
NM_001063.3:c.1461C>T	NP_001054.1:p.Tyr487=
XM_011513100.1:c.1461C>T	XP_011511402.1:p.Tyr487=
NM_001354703.1:c.1329C>T	NP_001341632.1:p.Tyr443=
NM_001354704.1:c.1080C>T	NP_001341633.1:p.Tyr360=
NM_001063.4:c.1461C>T MANE Select	NP_001054.2:p.Tyr487=
NM_001354703.2:c.1329C>T	NP_001341632.2:p.Tyr443=
NM_001354704.2:c.1080C>T	NP_001341633.2:p.Tyr360=